A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772199



Internal ID18962508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28510222..29115423hg38UCSC Ensembl
chr6:28477999..29083200hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38605202
hg19605202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074388
Supporting Variants
SamplesKWP1
Known GenesC6orf100, GPX5, GPX6, HCG14, LOC100129636, LOC401242, OR2B3, OR2J3, OR2W1, SCAND3, TRIM27, ZNF311
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772199
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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